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WO1999046346A1 - Agents de recouvrement et leur utilisation pour realiser des revetements constitues de plusieurs couches de laque - Google Patents

Agents de recouvrement et leur utilisation pour realiser des revetements constitues de plusieurs couches de laque Download PDF

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Publication number
WO1999046346A1
WO1999046346A1 PCT/EP1999/001553 EP9901553W WO9946346A1 WO 1999046346 A1 WO1999046346 A1 WO 1999046346A1 EP 9901553 W EP9901553 W EP 9901553W WO 9946346 A1 WO9946346 A1 WO 9946346A1
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Prior art keywords
meth
weight
functional
groups
components
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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PCT/EP1999/001553
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German (de)
English (en)
Inventor
Ralf Dahm
Carmen Flosbach
Hermann Kerber
Apostolos Manassis
Peter RÖSSIG
Walter Schubert
Astrid TÜCKMANTEL
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Axalta Coating Systems Germany GmbH and Co KG
EIDP Inc
Original Assignee
Herberts GmbH
EI Du Pont de Nemours and Co
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Application filed by Herberts GmbH, EI Du Pont de Nemours and Co filed Critical Herberts GmbH
Priority to EP99917818A priority Critical patent/EP1064337B1/fr
Priority to JP2000535714A priority patent/JP2002506114A/ja
Priority to DE59903465T priority patent/DE59903465D1/de
Priority to AT99917818T priority patent/ATE228153T1/de
Publication of WO1999046346A1 publication Critical patent/WO1999046346A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins

Definitions

  • the invention relates to coating compositions and their use in the production of multi-layer coatings, for example in the motor vehicle sector, in particular in the production of two-layer coatings of the basecoat / clearcoat type.
  • Coating agents which harden under esterification and are based on a combination of epoxy-functional component and carboxyl-functional component are known. They are characterized by the good chemical and acid resistance of the coatings created and baked from them and are therefore particularly suitable as clear or top coats in automotive OEM painting.
  • a stoving lacquer is known in which carboxyl-containing polymers, such as e.g. (Meth) acrylic copolymers based on acrylic acid or methacrylic acid and glycidyl group-containing acrylate resins are mixed to form a curable composition.
  • carboxyl-containing polymers such as e.g. (Meth) acrylic copolymers based on acrylic acid or methacrylic acid and glycidyl group-containing acrylate resins are mixed to form a curable composition.
  • DE-A-42 37 658 also describes stoving lacquer systems based on components containing carboxyl groups and components containing epoxy groups. Here the carboxyl groups are extended with lactone to increase the reactivity.
  • the optical-aesthetic impression of basecoat / clearcoat two-coat paint is significantly influenced by the quality of the clearcoat layer.
  • the structure of the clear lacquer layer on horizontal and vertical surfaces of a three-dimensional substrate, for example an automobile body is the same.
  • the ideal case described cannot easily be achieved.
  • it can form differences in the surface structure 2 or in the course of the outer clear lacquer layer, since the clear lacquers tend to run off or sag on surfaces outside the horizontal after their application and in particular during the heating phase during the stoving process as a result of a temperature-related reduction in viscosity.
  • urea compounds as anti-sagging agents in paints which contain hydroxy-functional binders and aminoplast resins or free or blocked polyisocyanates as crosslinking agents.
  • the chemical resistance, in particular the acid resistance, of the baked-on coating layers produced from these coating compositions is in need of improvement.
  • the object of the invention is to provide coating agents which have a reduced tendency to run off even when applied in higher layer thicknesses and which, when baked, lead to coatings with good acid and chemical resistance.
  • the coating agents are intended in particular as
  • Stoving coating agent for creating the outer clear or top coat layer of a multi-layer coating may be suitable.
  • curable coating compositions comprising binders and crosslinking agents, one or more organic solvents, anti-sagging agents, and, if appropriate, pigments and / or fillers and, if appropriate, other additives customary in lacquer, which are characterized in that 20 to 80 parts by weight or several carboxyl-functional components A) selected from carboxyl-functional (meth) acrylic copolymers and / or carboxy-functional polyesters, the carboxy functionality of which is in each case an acid number of 15 to 300 mg
  • KOH / g contains 20 to 80% by weight of one or more epoxy-functional crosslinkers B), the% by weight adding up to 100% by weight, where 3 components A) and B) can be at least partially precondensed and 5 to 30% by weight of one or more polymer polyols C), selected from hydroxyl-functional polyesters, polyurethanes and / or (meth) acrylic copolymers, of components A) which may contain hydroxyl groups and B) are different, based on the sum of the weight of components A) and B), and 0.1 to 3% by weight, based on the resin solid, of one or more previously in the presence of at least part of the or Polymer polyols C) produced or dispersed, solid urea compounds D) which are insoluble in the coating composition are present as anti-sagging agents, all the percentages by weight based on the solids content.
  • 3 components A) and B) can be at least partially precondensed and 5 to 30% by weight of one or more polymer polyols C), selected from
  • the binder / crosslinking system of the coating compositions according to the invention contains components A), B) and C) as essential components and, if appropriate, optional components E) and / or F) explained below.
  • the coating compositions according to the invention can only contain components A), B) and C) as a binder / crosslinking system, or the binder / crosslinking system of the coating compositions according to the invention additionally contains the optional components E) and / or F).
  • the resin solid of the coating compositions according to the invention is formed from the
  • the hardening of the coating compositions according to the invention is based on the chemical reaction of the complementarily reactive groups of components A) and B) taking place during the baking; it is an addition of the carboxyl to the epoxy groups with the formation of carboxylic acid ester bonds.
  • the present invention provides curable coating compositions with which the object can be achieved, although the hydroxyl groups of component C) of the coating compositions according to the invention are not 4 is only different from the complementary reactive, functional groups of components A) and B), but also non-complementary reactive groups.
  • the coating compositions according to the invention contain one or more carboxy-functional components A) as component A).
  • the carboxy-functional component A) of the coating compositions according to the invention are carboxy-functional (meth) acrylic copolymers and / or carboxy-functional polyesters, the carboxy functionality of which corresponds in each case to an acid number of 15 to 300 mg KOH / g.
  • the carboxy-functional (meth) acrylic copolymers and / or carboxy-functional polyesters can be urethanized and / or modified by reaction with lactones.
  • the carboxy-functionalized (meth) acrylic copolymers of component A) which optionally contain urethane groups preferably have a number average of
  • the carboxy-functionalized polyesters of component A) optionally containing urethane groups preferably have a calculated molecular weight of 500 to 4000 g / mol.
  • the acid number is in each case 15 to 300 mg KOH / g, preferably 30 to 250 mg KOH / g.
  • carboxyl group-containing (meth) acrylic copolymers or polyesters of component A), which may optionally each contain urethane groups the carboxyl groups can be introduced directly by using building blocks containing carboxyl groups.
  • suitable carboxyl group-containing monomers which can be used to build up carboxyl group-containing (meth) acrylic copolymers are unsaturated carboxylic acids, such as e.g. Acrylic, methacrylic, itaconic, croton, isoerotonic, aconitic, maleic and fumaric acid, half esters of maleic and fumaric acid and carboxyalkyl esters of (meth) acrylic acid, e.g. beta-carboxyethyl acrylate and adducts of hydroxyalkyl (meth) acrylates with
  • Carboxylic anhydrides such as, for example, the mono-2- (meth) acryloyloxyethyl phthalate.
  • (meth) acrylic is used in the present description and the claims. This means acrylic and / or methacrylic.
  • Ratios are worked that if necessary enough hydroxyl groups remain to be able to carry out a urethanization.
  • Suitable carboxylic anhydrides for the addition to the hydroxyl-containing polymers, which may already contain carboxyl groups, are
  • Anhydrides of di- and polycarboxylic acids such as, for example, preferably phthalic, tetrahydro, methylhexahydro and hexahydrophthalic anhydride.
  • Hydroxylalkyl (meth) acrylates such as e.g. Hydroxyethyl (meth) acrylate, and the hydroxypropyl (meth) acrylates and hydroxybutyl (meth) acrylates isomeric with respect to the position of the hydroxyl group.
  • hydroxy-functionalized component at least partially one can also
  • Reaction product from (meth) acrylic acid with the glycidyl ester of a carboxylic acid with a tertiary alpha carbon atom can be used.
  • Glycidyl esters of strongly branched monocarboxylic acids are available, for example, under the trade name "Cardura”.
  • the reaction of acrylic acid or methacrylic acid with the glycidyl ester of a carboxylic acid with a tertiary alpha carbon can take place before, during or after the polymerization reaction.
  • olefinically unsaturated monomers can also be used in the preparation of the (meth) acrylic copolymers of component A), in particular those which contain no further functional groups apart from an olefinic double bond.
  • the selection of the further olefinically unsaturated monomers is not critical; the olefinic monomers customary for polymerization can be used with or without further functional groups.
  • the monomers are preferably selected in a manner familiar to those skilled in the art so that their incorporation does not lead to undesirable properties of the copolymer.
  • Suitable further olefinically unsaturated monomers are, for example, in particular alkyl esters of (meth) acrylic acid which contain, for example, 1 to 20 C atoms or more in the alkyl part, such as e.g. Methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, isopropyl (meth) acrylate, isobutyl (meth) acrylate, tertiary butyl (meth) acrylate, hexyl (meth) acrylate,
  • alkyl esters of (meth) acrylic acid which contain, for example, 1 to 20 C atoms or more in the alkyl part, such as e.g. Methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate,
  • Cyclohexyl (meth) acrylate 2-ethylhexyl (meth) acrylate, decyl (meth) acrylate, hexadecyl (meth) acrylate.
  • alkyl esters of maleic, fumaric, tetrahydrophthalic, crotonic, isoerotonic, vinyl acetic and itaconic acid which contain, for example, 1 to 20 carbon atoms or more, e.g. the corresponding methyl, ethyl, propyl, butyl, isopropyl, isobutyl, pentyl, amyl, isoamyl, hexyl, cyclohexyl, 2-ethylhexyl, octyl, decyl, dodecyl ester.
  • monomers with at least two 7 polymerizable, olefinically unsaturated double bonds can be used.
  • the proportion of these monomers is preferably less than 5% by weight, based on the total weight of the monomers.
  • Another suitable component are monovinyl aromatic compounds.
  • styrene vinyl toluene, alpha-methyl styrene and the isomeric methyl styrenes. Vinyl toluenes and in particular styrene are preferably used. It is also possible to use silane-modified monomers, e.g. gamma-methacryloxypropyltrimethoxysilane.
  • the (meth) acrylic copolymers of carboxy-functional component A) are produced by radical copolymerization. It may prove advantageous to meter in some of the monomers at different times from one another.
  • the monomers or the monomer mixture used can contain radical initiators. If radical initiators are not contained in the monomer mixture, they can optionally be added to the monomer mixture with a slight time lag or added separately. You can then continue for a longer period, e.g. be polymerized for several hours. It is then possible to adjust to a desired solids content, for example in the order of 30 to 80% by weight, for example 50 to 60% by weight, using a conventional paint solvent.
  • radical initiators are dialkyl peroxides, diacyl peroxides, hydroperoxides, peresters, peroxide dicarbonates, perketals, ketone peroxides; Azo compounds, such as 2,2'-azo-bis- (2,4-dimethyl-valeronitrile), azo-bis-isobutyronitrile, CC-cleaving initiators such as, for example, benzpinacol derivatives.
  • the polymerization initiators are generally added, for example, in an amount of from 0 to 4% by weight, based on the weight of monomers.
  • hydroxyl groups of the carboxyl-functionalized (meth) acrylic copolymers of component A) can be reacted with mono-, di-, tri- or polyisocyanates in a further reaction step.
  • isocyanates which can be used for urethanization are phenyl isocyanate, and the polyisocyanates mentioned below in the description of the additional crosslinking agents E) and those which are substoichiometric by reaction with respect to the isocyanate content
  • Defunctionalization products available in amounts of monoalcohols available in amounts of monoalcohols.
  • the amount of di-, tri- or polyisocyanates used for urethanization is chosen in a manner familiar to the person skilled in the art so that gelling is avoided.
  • the carboxyl group-containing and optionally urethane group-containing polyesters of component A) can be built up according to customary methods from aliphatic and / or cycloaliphatic di-, tri- or higher alcohols, optionally together with monohydric alcohols and from aliphatic, aromatic and / or cycloaliphatic carboxylic acids, especially dicarboxylic acids, as well as higher quality polycarboxylic acids.
  • suitable alcohols are aliphatic diols, such as ethylene glycol, 1,2-propanediol, 1,3-propanediol, 2,2-diethyl-1,3-propanediol, the isomeric butanediols, 1,5-pentanediol, 3-methyl-1 , 5-pentanediol, 1,6-hexanediol, 2-
  • polyhydric aliphatic alcohols such as glycerol, trimethylolethane, 9 Ditrimethylolpropane, trimethylolpropane, pentaerythritol, and etherification products of diols and polyols, for example di- and triethylene glycol, polyethylene glycol, neopentyl glycol ester of hydroxypivalic acid
  • carboxylic acids examples include adipic, azelaic, 1,3 and 1,4.
  • the carboxyl-functionalized polyesters of component A) can be urethanized.
  • the reaction conditions and the polyisocyanates that can be used are the same as for the (meth) acrylic copolymers. It is possible to introduce the urethane groups by reacting the carboxyl- and hydroxyl-functional polyesters with mono-, di-, tri- or more highly functional ones
  • the carboxyl groups of the carboxy-functional (meth) acrylic copolymers and polyester of component A) can be "chain extended” with a lactone.
  • the "chain extension” results from the ring-opening addition of lactones to the carboxyl and / or hydroxyl groups. This creates terminal, exposed carboxyl or hydroxyl groups.
  • Lactones are preferably added to carboxy-functional (meth) acrylic copolymers and polyesters of component A) which are free from OH groups.
  • the lactone is preferably added last
  • the curable coating compositions according to the invention contain, as component B), one or more epoxy-functional crosslinking agents. These are, for example, compounds with at least two epoxy functions in the molecule and an epoxy equivalent weight of, for example, 200 to 700, preferably 250 to 500 and in particular 300 to 400, in each case based on solid resin.
  • the number average molecular weight (Mn) is preferably 200 to 10,000 g / mol.
  • the glass transition temperature is preferably from -20 ° C to 70 ° C, particularly preferably from 0 ° C to 50 ° C and in particular from 5 ° C to 40 ° C.
  • the upper limit is preferably up to 50 ° C.
  • Examples of these are common di- or polyepoxides, e.g. Polyglycidyl ether based on diethylene glycol, dipropylene glycol, polypropylene glycol, bisphenol A or triglycidyl ether of glycerin.
  • di- or polyepoxides are those based on di- or polyglycidyl esters.
  • examples of these are reaction products of l-hydroxy-2,3-epoxypropane with phthalic or terephthalic acid to give phthalic or terephthalic acid bis (2,3-epoxypropyl ester) or a diglycidyl ether of bisphenol A with trimellitic anhydride to give polyesters, for example with a number average of
  • Preferred components B) are epoxy-functional (meth) acrylic copolymers, in particular glycidyl (meth) acrylate copolymers.
  • comonomers for example (meth) acrylic acid esters, e.g. Methyl, ethyl, butyl, isobutyl,
  • Ethylhexyl, cyclohexyl and / or lauryl (meth) acrylate can be selected, (meth) acrylic acid hydroxyalkyl esters such as e.g. Hydroxyethyl and / or hydroxypropyl (meth) acrylate, also styrene, vinyl toluene and / or alpha-methyl styrene and all alpha, beta-unsaturated monomers, as already described above for component A).
  • Molecular weight can be, for example, between 1000 and 10,000, preferably between 2000 and 5000.
  • Other copolymerizable glycidyl-functional monomers are 11 for example (meth) allyl glycidyl ether or 3,4-epoxy-1-vinylcyclohexane.
  • the copolymers are prepared by free-radical solution polymerization, they are known to the person skilled in the art and require no further explanation.
  • precondense components A) and B) at least partially in a further reaction step can e.g. done by heating components A) and B) together.
  • the desired degree of condensation can be determined, for example, by reducing the acid number. For example, it is possible to heat to temperatures of, for example, 80 to 120 ° C. with stirring and continue to stir until the
  • the acid number of the mixture has dropped by, for example, 2 to 5 mg KOH / g solid resin.
  • the proportions are preferably chosen so that a molar ratio of the carboxyl to epoxide groups of 1: 3 to 3: 1 is present between the carboxyl group-containing component A) and the epoxy component B).
  • the coating compositions of the invention each contain, based on the solids content, 5 to 30% by weight, preferably 5 to 20% by weight, of one or more polymer polyols C), based on the sum of the weights of components A) and B). Some or all of the amount of the polymer polyol (s) C) present in the coating compositions of the invention serves as the reaction medium in the
  • the polymer polyols C) are polymer polyols selected from hydroxymotional polyesters, polyurethanes and / or (meth) acrylic copolymers, which are different from components A) and B) which may contain hydroxyl groups.
  • the polymer polyols C) have at least two hydroxyl functions in the molecule.
  • the polymer polyols C) can also contain carboxyl groups corresponding to an acid number of 0 to 15 mg KOH / g.
  • the polymer polyols C) preferably contain no further functional groups, in particular no epoxy groups.
  • the polymer polyols used in the coating compositions according to the invention have, for example, a number average molecular weight (Mn) of 500 to 10,000 and a hydroxyl number of 30 to 350 mg KOH / g.
  • hydroxy-functional polyester resins which can preferably be used as polymer polyols C) in the coating compositions according to the invention are conventional, for example those with a number average molecular weight (Mn) of 500 to 5000, preferably from 1000 to 3000 and hydroxyl numbers from 30 to 350, preferably from 50 to 280 mg KOH / g.
  • Mn number average molecular weight
  • hydroxy-functional polyurethane resins which can preferably be used as polymer polyols C) in the coating compositions according to the invention are customary, for example those with a number average molecular weight (Mn) of 500 to 5000, preferably from 1000 to 3000 and hydroxyl numbers from 30 to 350, preferably from 50 to 280 mg KOH / g.
  • Mn number average molecular weight
  • hydroxy-functional (meth) acrylic copolymers which can preferably be used as polymer polyols C) in the coating compositions according to the invention are customary, for example those with a number average molecular weight (Mn) between 1000 and
  • the (meth) acrylic copolymers can, for example, have been prepared in the presence of oligomeric or polymeric polyester and / or polyurethane resins, for example those as explained in the two preceding paragraphs.
  • the coating compositions according to the invention can also contain one or more additional epoxy crosslinkers B) Contain 13 different crosslinkers E), which allow additional crosslinking with the inclusion of hydroxyl groups, for example the hydroxyl groups present in the binder system and / or formed during the baking in the course of the epoxy / carboxyl addition reaction.
  • the additional crosslinkers are present in proportions of a total of 0 to 20% by weight, based on the sum of components A), B) and C), in each case based on the solids content.
  • additional crosslinking agents E) are aminoplast resins, in particular melamine resins.
  • examples include melamine resins etherified with butanol or isobutanol, e.g. the
  • additional crosslinking agents E) are triazine-based components which crosslink to form ester groups, in particular with the formation of urethane groups (carbamic acid ester groups), such as, for example, preferably tris (alkoxycarbonylamino) triazine.
  • additional crosslinking agents E) are blocked polyisocyanates which can be prepared from free polyisocyanates by reaction with compounds containing an active hydrogen atom which can be split off under the baking conditions.
  • polyisocyanates that can be used are, in particular, cycloaliphatic and aliphatic polyisocyanates such as tetramethylene diisocyanate,
  • the known polyisocyanates which are usually used in the production of paints, are particularly well suited, e.g. Biuret, isocyanurate or
  • Modification products containing urethane groups of the simple polyisocyanates mentioned above in particular tris (6-isocyanatohexyl) biuret, the isocyanurate derived from isophorone diisocyanate or hexane diisocyanate or low molecular weight polyisocyanates containing urethane groups, such as those obtained by reacting excess isophorone diisocyanates with the molecular weight range of simple polyvalent alcohols 62 to 300, especially with trimethylolpropane can be obtained. Any mixtures of the polyisocyanates mentioned can of course also be used.
  • Suitable polyisocyanates are also the known prepolymers containing terminal isocyanate groups, as are accessible in particular by reacting the simple polyisocyanates mentioned above, especially diisocyanates, with inadequate amounts of organic compounds having at least two groups which are reactive toward isocyanate groups.
  • the ratio of isocyanate groups to hydrogen atoms reactive towards isocyanate groups preferably corresponds to 1.05 to 10: 1, particularly preferably 1.1 to 3: 1, the hydrogen atoms preferably originating from hydroxyl groups.
  • the nature and proportions of the starting materials used in the preparation of prepolymers containing isocyanate groups are preferably chosen so that the prepolymers containing isocyanate groups have an average NCO functionality of 2 to 4, preferably 2 to 3 and a number average molecular weight (Mn) of 500 to 10,000, preferably from 800 to 4000.
  • Customary capping agents are used, for example compounds with an active hydrogen atom, selected from CH-acidic compounds such as acetylacetone or CH-acidic esters, such as, for example, alkyl acetoacetate, 15 malonic acid dialkyl esters, aliphatic or cycloaliphatic alcohols, such as n-butanol, isopropanol, tert.
  • CH-acidic compounds such as acetylacetone or CH-acidic esters, such as, for example, alkyl acetoacetate, 15 malonic acid dialkyl esters, aliphatic or cycloaliphatic alcohols, such as n-butanol, isopropanol, tert.
  • additional crosslinking agents E which may be present in the coating compositions according to the invention are organic compounds which have at least two cyclic carboxylic anhydride groups per molecule.
  • the content of carboxylic acid anhydride groups in these compounds (formally calculated as C 4 0 3 ,
  • trimellitic anhydride esters of ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, neopentyl glycol, glycerol or trimethylolpropane are preferred, preferably prepared in the ratio of 1 mol of trimellitic anhydride per mol of hydroxyl groups.
  • polyanhydrides are, for example, benzophenonetetracarbonic acid dianhydride and 1,2,4,5-benzene tetracarboxylic acid dianhydride.
  • Particularly preferred polyanhydrides are copolymers of olefinically unsaturated
  • Monomers which have at least two cyclic carboxylic anhydride groups on average per molecule are preferably copolymers of maleic anhydride and / or itaconic anhydride with conventional comonomers, as described, for example, in connection with component A).
  • Copolymers based on maleic anhydride, styrene and / or alkyl esters of acrylic and / or methacrylic acid are particularly suitable.
  • the copolymers preferably have a number average molecular weight (Mn) of 1,500 to 75,000, preferably 2,000 to 50,000.
  • the coating compositions according to the invention can contain 0 to 10% by weight of one or more monoepoxide compounds F), based on the sum of components A) and B), in each case based on the solid.
  • the baking conditions essentially non-volatile substances, for example the volatile content is preferably less than 1 wt .-%, based on the total amount of monoepoxide F).
  • the molar masses of the monoepoxides F) are above 150 and such compounds with an average molecular weight of up to 3000, particularly preferably below 1000, are preferred. In the case of the low molecular weights, these compounds can have a positive influence on the viscosity behavior of the lacquers produced thereby, since they add up Carboxyl groups of component A) act as reactive diluents.
  • Diglycidyl compound e.g. a diglycidyl ether, such as one mole of bisphenol A diglycidyl ether and one mole of a saturated or unsaturated monocarboxylic acid such as acetic acid, propionic acid or isononanoic acid.
  • reaction products of di- or polyepoxides such as e.g. Polyglycidyl ether based on diethylene glycol, dipropylene glycol, polypropylene glycol with a
  • Mw Number average molecular weight (Mw) of up to 2000 and triglycidyl ether of glycerol and / or polyphenols such as bisphenol A or F with the monocarboxylic acids mentioned.
  • the glycidyl ester of versatic acid with is particularly preferred
  • the coating compositions according to the invention have, for example, a solids content, formed from the resin solids, the urea compounds D) explained below and any further nonvolatile constituents which may be present, from 40 to 70% by weight.
  • volatile constituents they contain organic solvents such as are customary, for example, for the production of coating agents, for example paints. Solvents can also be used, such as are used in the production of the individual components. Examples are glycol ethers, such as butyl glycol, butyl diglycol,
  • Dipropylene glycol dimethyl ether dipropylene glycol monomethyl ether, ethylene glycol dimethyl ether; Glycol ether esters, such as ethyl glycol acetate, 17
  • the coating compositions according to the invention contain 0.1 to 3, preferably 0.3 to 2, particularly preferably 0.5 to 1.5% by weight, based on the resin solids
  • Coating agents one or more solid urea compounds D) which have been prepared beforehand in the presence of at least part of the polymer polyol (s) C) as an anti-sagging agent, i.e. as thixotropic or structural viscosity agents which have a favorable effect on the runoff behavior of the coating compositions according to the invention. They effectively prevent the unwanted draining or sagging of coating layers applied from the coating compositions according to the invention to vertical surfaces.
  • the urea compounds D) are known as anti-sag agents, for example from DE-C-27 51 761, EP-A-0 192 304 and EP-A-0 198 519.
  • the urea compounds D) are addition products made from aromatic, araliphatic, cycloaliphatic or aliphatic diisocyanates and / or polyisocyanates derived therefrom (for example those derived from isocyanurate
  • urea compounds D) are those in which polyisocyanate and amine have been reacted in a stoichiometric ratio of 0.7-1.5 primary and / or secondary amino groups per isocyanate group, particularly preferably in a stoichiometric ratio of amino groups 18th
  • Particularly preferred urea compounds D) are addition products from diisocyanates, preferably from aliphatic or cycloaliphatic diisocyanates and primary amines, preferably primary monoamines.
  • the aliphatic or cycloaliphatic diisocyanates are preferably symmetrically structured diisocyanates.
  • the urea compounds D) used in the coating compositions according to the invention are selected so that they are solid, particularly preferably crystalline substances.
  • the particle sizes of the D) particles are preferably 0.1 to 20 ⁇ m.
  • the solid or crystalline urea compounds D) preferably have a high one
  • Solidification or melting point which is in particular above the baking temperatures prevailing when the coating compositions of the invention are baked, in particular above 80 ° C., for example between 80 and 250 ° C.
  • the adduct formed from 1 mol of 1,6-hexane diisocyanate and 2 mol of benzylamine is particularly preferably used as the urea compound D) in the coating compositions according to the invention.
  • the urea compounds D) can be prepared in a conventional manner by adding amines with primary and / or secondary amino groups to polyisocyanates.
  • Amine can be added to the polyisocyanate or polyisocyanate to the amine, or the reactants are added simultaneously, the addition of the polyisocyanate to the amine being preferred.
  • the preparation takes place, for example, at temperatures between 20 and 80 ° C. in the presence of at least some of the polymer polyols C) present in the coating agent according to the invention, ie in the presence of some or all of the hydroxy-functional polymer polyol component C) present in the coating agent according to the invention.
  • the reaction system prefferably be thoroughly mixed, for example by vigorous stirring, by using a dissolver or by carrying out the addition reaction in or using a rotor-stator unit.
  • the coating agent according to the invention contains more than one polymer polyol C), it can be produced, for example, in one of these polymer polyols C). It is preferred to work in such a way that the urea compounds D) formed in the polymer polyol component C) or in the dissolved polymer polyol component C) 19 finely divided solid precipitate or crystallize out, for example during or after the end of the addition reaction, for example during or after cooling.
  • Such dispersions of urea compounds D) present as a finely divided, preferably crystalline solid in the polymer polyol component C) or its solution can also be prepared by melting and finely distributing the urea compounds D) in C) and then cooling below the solidification or melting point of the urea compounds D. ).
  • the content of the urea compounds D) in the dispersions is, for example, 0.5 to 10, in particular between 1 and 10,% by weight, based on the solids content of polymer polyol C).
  • the coating compositions of the invention are preferably prepared such that the dispersion of the urea compounds D) in the liquid or dissolved polymer polyol C) is mixed with the other constituents of the coating composition.
  • components A) and B) are first mixed before the other constituents are added.
  • urea compounds D which can be used in the coating compositions according to the invention, starting materials, processes and process parameters for
  • compositions of the invention are intended as pigmented topcoats, for example in the production of the outer top layer
  • Multi-layer painting are used, they contain pigments and fillers if necessary.
  • the pigment / resin solids weight ratio is, for example, in the range between 0.05 to 2: 1.
  • pigments are inorganic and / or organic colored pigments and / or effect pigments, such as e.g. Titanium dioxide, iron oxide pigments, carbon black, azo pigments, phthalocyanine pigments,
  • Quinacridone pigments metal pigments, for example made of titanium, aluminum or copper, interference pigments, such as, for example, titanium dioxide-coated aluminum 20 mica, graphite effect pigments, platelet-shaped iron oxide, platelet-shaped copper pthalocyanine pigments.
  • fillers are standard fillers, such as talc and silicates.
  • the pigmented topcoats or preferably as transparent
  • customary lacquer additives in quantities customary in lacquer, for example up to 5% by weight, based on the entire lacquer, e.g. transparent pigments or fillers, leveling agents, dyes, light stabilizers, antioxidants or other rheology controllers which can be used in addition to the urea compounds D
  • the coating compositions according to the invention can be applied by known methods, in particular by spraying in layer thicknesses, for example from 25 to 60 ⁇ m. After an evaporation phase, the applied coating agent is crosslinked by heating.
  • the baking temperatures are e.g. at 60 to 180 ° C, preferably at 60 to 160 ° C.
  • the coating compositions of the invention can be used, for example, to produce the outer pigmented topcoat layer of a multi-layer coating.
  • the present invention also relates to the use of the coating compositions of the invention as topcoat compositions.
  • the coating compositions according to the invention are preferably formulated as transparent clear lacquers which can be used to produce the outer clear lacquer layer of a multi-layer lacquer.
  • the present invention also relates to the use of the coating compositions according to the invention as
  • the clear lacquer coating composition according to the invention can be used with or with a coloring and / or effect 21 multi-layer pre-coated substrate can be applied and baked.
  • the stoving temperatures of the clear lacquer coating compositions according to the invention are, for example, between 60 and 160 ° C.
  • For automotive applications they are, for example, between 60 and 140, for applications in automotive OEM painting in particular between 80 and 140 and preferably between 110 and 130 ° C.
  • the clear lacquer coating compositions according to the invention are preferably used for producing a basecoat / clearcoat multi-layer coating.
  • a coloring and / or effect-imparting basecoat layer is applied to an optionally precoated substrate, in particular to precoated automobile bodies or parts thereof, before the clearcoat coating layer is applied from a clearcoat coating agent according to the invention and baked.
  • pre-coatings on automobile bodies or their parts are an electrocoat layer, a two-layer pre-coat consisting of an electrocoat layer and a spray filler layer or a two-layer pre-coat consisting of an electrocoat layer and a second electrophoretically applied coating layer.
  • the color and / or effect basecoat can be applied before
  • Clear coat from the clear coat coating composition according to the invention are baked, but preferably the clear coat coating composition according to the invention is applied by the known wet-on-wet process to the basecoat layer determining the color tone of the multi-layer coating.
  • the basecoat film is applied by spraying from a color and / or effect aqueous or solvent-based basecoat in a dry film thickness depending on the color, for example between 10 and 25 ⁇ m.
  • a short flash-off phase e.g. at 20 to 80 ° C
  • the application of the clear coat from the clear coat composition according to the invention for example by spraying, for example in a
  • Dry layer thickness of generally between 25 and 50 microns. If necessary, it can be vented briefly.
  • the substrate is then fed to the baking process at 22 the clear coat layer is baked together with the basecoat at elevated temperatures, for example from 60 to 160 ° C.
  • the present invention can be used to produce multi-layer coatings, in particular basecoat / clearcoat two-layer coatings, in particular on motor vehicles and their parts with an excellent aesthetic impression and good chemical and acid resistance. A run-off of the clear varnish on vertical surfaces during curing, especially baking, is effectively prevented.
  • the product has a stoving residue of 64.5% (1H, 150 ° C) and a hydroxyl number of 390 mg KOH / g, based on the solids content.
  • the carboxyl-functional polyester resin has a stoving residue of 67.7% (lh 23 150 ° C) and an acid number of 190 mg KOH / g, based on the solids content.
  • Example 2 a - c production of clearcoats and production of multi-layer coatings
  • a black basecoat in a dry layer thickness of 16 ⁇ m is sprayed onto sheets provided with a cataphoresis primer and filler layer and pre-dried at 80 ° C for 10 minutes.
  • the clear coats 2 a - c are each sprayed onto the hanging sheets in a wedge shape in a dry layer thickness of 10 to 60 ⁇ m. After 5 minutes flashing off at room temperature, it is baked for 20 minutes at 140 ° C (object temperature). The sheets are in the vertical position during all operations.
  • Table 1 shows their respective

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne des agents de recouvrement pouvant être utilisés pour réaliser un revêtement constitué de plusieurs couches de laque, qui comprennent des solvants organiques et, comme liant, 20 à 80 % en poids de copolymères (méth)acrylique et/ou de polyesters A) à fonction carboxy, dont la fonctionnalité carboxy correspond chaque fois à un indice d'acidité de 15 à 300 mg KOH/g, et 20 à 80 % en poids de réticulant B) à fonction époxyde, les composants A) et B) pouvant être, au moins partiellement, précondensés, ainsi que 5 à 30 % en poids de polyesters, de polyuéthanes et/ou de copolymères (méth)acrylique C) à fonction hydroxyle, par rapport à la somme des pourcentages en poids des composants A) et B), et 0,1 à 3 % en poids de composés d'urée solides, non solubles dans l'agent de recouvrement, préalablement produits ou dispersés en présence d'au moins une partie du ou des composants C).
PCT/EP1999/001553 1998-03-10 1999-03-05 Agents de recouvrement et leur utilisation pour realiser des revetements constitues de plusieurs couches de laque Ceased WO1999046346A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP99917818A EP1064337B1 (fr) 1998-03-10 1999-03-05 Agents de recouvrement et leur utilisation pour realiser des revetements constitues de plusieurs couches de laque
JP2000535714A JP2002506114A (ja) 1998-03-10 1999-03-05 塗料剤および多層ラッカーコーティングの製造におけるその使用
DE59903465T DE59903465D1 (de) 1998-03-10 1999-03-05 Überzugsmittel und deren verwendung zur herstellung von mehrschichtlackierungen
AT99917818T ATE228153T1 (de) 1998-03-10 1999-03-05 Überzugsmittel und deren verwendung zur herstellung von mehrschichtlackierungen

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19810219A DE19810219C2 (de) 1998-03-10 1998-03-10 Überzugsmittel und deren Verwendung zur Herstellung von Mehrschichtlackierungen
DE19810219.4 1998-03-10

Publications (1)

Publication Number Publication Date
WO1999046346A1 true WO1999046346A1 (fr) 1999-09-16

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PCT/EP1999/001553 Ceased WO1999046346A1 (fr) 1998-03-10 1999-03-05 Agents de recouvrement et leur utilisation pour realiser des revetements constitues de plusieurs couches de laque

Country Status (5)

Country Link
EP (1) EP1064337B1 (fr)
JP (1) JP2002506114A (fr)
AT (1) ATE228153T1 (fr)
DE (2) DE19810219C2 (fr)
WO (1) WO1999046346A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10122390A1 (de) * 2001-05-09 2002-11-28 Basf Coatings Ag Carbamat-und/oder Allophanatgruppen enthaltende, thermisch härtbare, thixotrope Gemische

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3022996B1 (de) * 1980-06-20 1981-04-02 Basf Farben + Fasern Ag, 2000 Hamburg Einbrennlack
EP0442336A2 (fr) * 1990-02-10 1991-08-21 Hoechst Aktiengesellschaft Agent de suspension pour mélanges liquides durcissables
JPH05132636A (ja) * 1991-11-12 1993-05-28 Dainippon Ink & Chem Inc 被覆膜の形成方法
JPH05168204A (ja) * 1991-12-13 1993-07-02 Toshiba Corp 誘導電動機の固定子の製造方法
DE4236901A1 (de) * 1992-10-31 1994-05-05 Herberts Gmbh Als Rheologie-Beeinflusser geeignete Zusammensetzung, Verfahren zu deren Herstellung und deren Verwendung in Überzugsmitteln
DE4237658A1 (de) * 1992-11-07 1994-05-11 Herberts Gmbh Bindemittelzusammensetzung, diese enthaltende Überzugsmittel, deren Herstellung und Verwendung
DE4310413A1 (de) * 1993-03-31 1994-10-06 Basf Lacke & Farben Nichtwäßriger Lack und Verfahren zur Herstellung einer zweischichtigen Decklackierung
WO1995027012A1 (fr) * 1994-04-04 1995-10-12 Ppg Industries, Inc. Dispersions non aqueuses de microparticules a fonction acide carboxylique utilisables pour le controle de debit dans les compositions de revetements a base de polyepoxyde-polyacide

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3022996B1 (de) * 1980-06-20 1981-04-02 Basf Farben + Fasern Ag, 2000 Hamburg Einbrennlack
EP0442336A2 (fr) * 1990-02-10 1991-08-21 Hoechst Aktiengesellschaft Agent de suspension pour mélanges liquides durcissables
JPH05132636A (ja) * 1991-11-12 1993-05-28 Dainippon Ink & Chem Inc 被覆膜の形成方法
JPH05168204A (ja) * 1991-12-13 1993-07-02 Toshiba Corp 誘導電動機の固定子の製造方法
DE4236901A1 (de) * 1992-10-31 1994-05-05 Herberts Gmbh Als Rheologie-Beeinflusser geeignete Zusammensetzung, Verfahren zu deren Herstellung und deren Verwendung in Überzugsmitteln
DE4237658A1 (de) * 1992-11-07 1994-05-11 Herberts Gmbh Bindemittelzusammensetzung, diese enthaltende Überzugsmittel, deren Herstellung und Verwendung
DE4310413A1 (de) * 1993-03-31 1994-10-06 Basf Lacke & Farben Nichtwäßriger Lack und Verfahren zur Herstellung einer zweischichtigen Decklackierung
WO1995027012A1 (fr) * 1994-04-04 1995-10-12 Ppg Industries, Inc. Dispersions non aqueuses de microparticules a fonction acide carboxylique utilisables pour le controle de debit dans les compositions de revetements a base de polyepoxyde-polyacide

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch Week 9326, Derwent World Patents Index; Class A82, AN 93-208944, XP002109990 *
DATABASE WPI Section EI Week 9331, Derwent World Patents Index; Class V06, AN 93-247387, XP002109989 *

Also Published As

Publication number Publication date
EP1064337B1 (fr) 2002-11-20
DE59903465D1 (de) 2003-01-02
ATE228153T1 (de) 2002-12-15
EP1064337A1 (fr) 2001-01-03
JP2002506114A (ja) 2002-02-26
DE19810219A1 (de) 1999-09-16
DE19810219C2 (de) 2001-04-12

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